Eurofins

Assistant Director - Genetic toxicology

Bengaluru, KA, IN

In-personFull time roleSenior Level, Director / Executive

4 months ago

About the Job

Experience (years)

20-22+ years relevant experience or PhD in Microbiology with at least 15+ years of relevant industry experience.

Job description:

  • In-depth scientific expertise in Genotoxicology, with significant experience in designing, executing, and interpreting genetic toxicology studies in both regulatory (FDA, EMA, ICH, and OECD guidelines) and non-regulatory environments.
  • Responsible for the execution, planning, performance, reporting/archiving, and management of studies such as the Bacterial Reverse Mutation Test (Ames Test), Bone Marrow Micronucleus Test, Chromosome Aberration Test, and In Vitro Micronucleus Test etc.
  • Preparation of study plans, protocols, amendments to study plans, study reports, creation, and review of SOPs.
  • Lead and manage a team of genetic toxicologists, providing mentorship and guidance to achieve departmental and organizational objectives.
  • Oversee study directors across multiple studies and ensure consistent performance.
  • Train and onboard new staff, ensuring they meet expected proficiency levels for quality work in compliance with GLP standards.
  • Prepare monthly forecasts and reports, and plan for the effective use of resources.
  • Focus on maintaining strong client communication, ensuring timely delivery of services, and fostering repeat business.
  • Oversee laboratory maintenance, equipment validation and calibration, and procurement of reagent supplies.
  • Participate in GLP/NABL activities, inspections, and ensure adherence to regulatory compliance guidelines; address Quality Assurance checklists and GLP compliance.
  • Collaborate with HOS/HOD in budgeting, costing, planning, and conducting studies, as well as in the development of new platforms and operational activities.
  • Support to business development and marketing efforts, generate new business leads alongside the BD team.
  •  Standardize and implement new in vitro test procedures.

Qualifications / Skills Required:

  • Masters in Microbiology (M.V.Sc / M.Sc) with at least 20-22+ years of relevant industry experience or PhD in Microbiology with at least 15+ years of relevant industry experience
  • Understanding of the agrochemical and pharmaceutical R&D process
  • Strong problem-solving skills and the ability to develop innovative solutions.
  • Experience in managing internal and external collaborations.
  • Willingness to adapt to rapidly changing scientific and regulatory environments.
  • Effective team collaboration skills to achieve project goals, objectives, and deadlines.

Behavioral Competencies:

  • Strong oral and written communication skills.
  • Ability to adapt and work efficiently in a dynamic environment.
  • Excellent time management skills to effectively handle multiple projects.
  • Highly motivated, takes responsibility for personal improvement, learning from experience and new situations.
  • Strong training, presentation, analytical, and computer skills
  • Thinks of and/or encourages new ideas and keen to experiment and see ideas implemented.

About the Company

Eurofins Logo

Eurofins

Luxembourg, Luxembourg

5000 +

<div class="org-about-module__description"> <div id="ember58" class="ember-view organization-about-module__content-consistant-cards-description"><span class="lt-line-clamp__raw-line">Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is a global leader in food, environmental, pharmaceutical and cosmetic product testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. Since 1987, Eurofins has grown from one laboratory in Nantes, France to ca. 62,000 staff across a network of independent companies in 62 countries, operating over 900 laboratories. Performing over 450 million tests every year, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Ever since its IPO on the French stock exchange in 1997, Eurofins has been one of the fastest growing listed European companies.</span></div> </div> <div class="org-about-module__content-improvement"> <div class="org-about-module__content-box">&nbsp;</div> </div>

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